APNEA GUARD


Device Classification Name

device, anti-snoring

510(k) Number K111110
Device Name APNEA GUARD
Applicant
ADVANCED BRAIN MONITORING, INC.
24301 woodsage drive
bonita springs, 
FL 
34134

Applicant Contact paul dryden
Correspondent
ADVANCED BRAIN MONITORING, INC.
24301 woodsage drive
bonita springs, 
FL 
34134

Correspodent Contact paul dryden
Regulation Number 872.5570
Classification Product Code
LRK  
Date Received 04/20/2011
Decision Date 07/22/2011
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Dental

510k Review Panel

Dental

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No